Variant (rsID / SNP)

rs476569

rs476569 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to C9. Location: chromosome 5, position 39,342,308. Clinical significance in the table: Benign.

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Reference-table entries

C9Benign

Clinical significance (as recorded): Benign
Variant type: single nucleotide variant
Chromosome / position: 5:39342308
Cytoband: 5p13.1
HGVS: NM_001737.5(C9):c.78-10G>A
Allele change: Silent

Public references

dbSNP
ClinVar
Ensembl
gnomAD

Classifications are reproduced unchanged from the reference table. For education only; not a substitute for medical or genetic counselling.